An adapter apparatus (24, 80) for a respiratory therapy system (2) having a pressure generating device (4) and an electrical tube assembly (22) coupled to a patient interface device (8) includes a first end having a first port member (66, 94) structured to be fluidly coupled to the electrical tube assembly, a second end having a second port member (70, 88) structured to receive a flow of breathing gas generated by the pressure generating device, the adapter apparatus being structured to deliver the flow of breathing gas to the electrical tube assembly through the first port member, and a wire assembly having a first electrical connector (76, 104) structured to be electrically coupled to the electrical tube assembly and a second electrical connector structured to be electrically coupled to the pressure generating device in order to provide an electrical connection between the electrical tube assembly and the pressure generating device.
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1. An adapter apparatus for a respiratory therapy system having a pressure generating device and an electrical tube assembly coupled to a patient interface device, the pressure generating device including an outlet port having a first housing having a first mating member structured to be mated with a second mating member of the electrical tube assembly to allow the electrical tube assembly to be connected to the first housing, the adapter apparatus comprising:
a first end having a first port member structured to be fluidly coupled to the electrical tube assembly;
a second end having a second port member structured to receive a flow of breathing gas generated by the pressure generating device, the adapter apparatus being structured to deliver the flow of breathing gas to the electrical tube assembly through the first port member;
a wire assembly having a first electrical connector structured to be electrically coupled to the electrical tube assembly and a second electrical connector structured to be electrically coupled to the pressure generating device in order to provide an electrical connection between the electrical tube assembly and the pressure generating device;
a third mating member having a configuration that matches a configuration of the first mating member, the third mating member being structured to be mated with the second mating member of the electrical tube assembly to allow the electrical tube assembly to be connected to the adapter apparatus; and
a connector housing, wherein the first electrical connector is received and held within the connector housing, wherein the first port member, the second port member and the connector housing are provided as part of a fluid coupling member, and wherein the fluid coupling member includes a housing that covers the connector housing and receives and holds at least a portion of the wire assembly.
7. A respiratory therapy system, comprising:
a pressure generating device structured to generate a flow of breathing gas, the pressure generating device including an outlet port having a first housing having a first electrical connector and a first mating member;
a patient interface device;
an electrical tube assembly coupled to the patient interface device at a distal end thereof, the electrical tube assembly having a second housing provided at a proximal end thereof, the second housing having a second electrical connector and a second mating member, wherein the second electrical connector is structured to be coupled to the first electrical connector to allow power and/or control signals to be provided to the electrical tube assembly from the pressure generating device and wherein the second mating member is structured to be mated with the first mating member to allow the second housing to be connected to the first housing; and
an adapter apparatus provided between the pressure generating device and the electrical tube assembly, the adapter apparatus including:
a first end having a first port member fluidly coupled to the electrical tube assembly;
a second end having a second port member structured to receive the flow of breathing gas, the adapter apparatus being structured to deliver the flow of breathing gas to the electrical tube assembly through the first port member;
a wire assembly having a third electrical connector electrically coupled to the second electrical connector of the electrical tube assembly and a fourth electrical connector electrically coupled to the first electrical connector of the pressure generating device to thereby provide an electrical connection between the electrical tube assembly and the pressure generating device; and
a third mating member having a configuration that matches a configuration of the first mating member, the third mating member being mated with the second mating member of the electrical tube assembly to connect the second housing to the adapter apparatus, wherein the adapter apparatus further comprises a connector housing, wherein the third electrical connector is received and held within the connector housing, and wherein the first port member, the second port member and the connector housing are provided as part of a fluid coupling member, and wherein the fluid coupling member includes a housing that covers the connector housing and receives and holds at least a portion of the wire assembly.
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This application is the U.S. National Phase application under U.S.C. § 371 of International Application Serial No. PCT/IB2013/061037, filed on Dec. 17, 2013, which claims the benefit of U.S. Application Ser. No. 61/740,217, filed on Dec. 20, 2012. These applications are hereby incorporated by reference herein.
1. Field of the Invention
The present invention pertains to systems for treating conditions, such as sleep disordered breathing, using positive airway pressure (PAP) therapy, and, in particular, to an inline adapter for a pressure support device that also allows for an electrical connection to be made between electrical (e.g., heated tubing) and the pressure support device.
2. Description of the Related Art
There are numerous situations where it is necessary or desirable to deliver a flow of breathing gas non-invasively to the airway of a patient, i.e., without intubating the patient or surgically inserting a tracheal tube into the patient's esophagus. For example, it is known to ventilate a patient using a technique known as non-invasive ventilation. It is also known to deliver positive airway pressure (PAP) therapy to treat certain medical disorders, the most notable of which is OSA. Known PAP therapies include continuous positive airway pressure (CPAP), wherein a constant positive pressure is provided to the airway of the patient in order to splint open the patient's airway, and variable airway pressure, wherein the pressure provided to the airway of the patient is varied with the patient's respiratory cycle. Such therapies are typically provided to the patient at night while the patient is sleeping.
Non-invasive ventilation and pressure support therapies as just described involve the placement of a patient interface device including a mask component having a soft, flexible sealing cushion on the face of the patient. The mask component may be, without limitation, a nasal mask that covers the patient's nose, a nasal/oral mask that covers the patient's nose and mouth, or a full face mask that covers the patient's face. Such patient interface devices may also employ other patient contacting components, such as forehead supports, cheek pads and chin pads. The patient interface device is connected to a gas delivery tube or conduit and interfaces the ventilator or pressure support device with the airway of the patient, so that a flow of breathing gas can be delivered from the pressure/flow generating device to the airway of the patient. It is known to maintain such devices on the face of a wearer by a headgear having one or more straps adapted to fit over/around the patient's head.
Some patients that use non-invasive ventilation and/or pressure support therapy devices have a need to add an inline accessory to the flow path of the device. Such accessories may include, for example and without limitation, oxygen enrichment adapters, pressure valves and bacteria filters. In addition, many patients are now using heated tubes in the flow path. Such heated tubes require an electrical connection to be made between a connector on the tube cuff and a connector near/on the outlet port of the ventilator or pressure support device. The requirement for such an electrical connection, however, makes it difficult to also use an inline accessory.
In the specific context of supplemental oxygen, in the prior art, in order to maintain heated tubing functionality while simultaneously receiving supplemental oxygen, the oxygen must be introduced to the patient at the mask side of the patient circuit, either directly into the mask or into an enrichment adapter provided between the mask and the main delivery conduit. This adds bulk to the mask and/or forces the patient to have additional tubing running to their face. This can reduce the comfort of the therapy experience, and thus may lease to decreased therapy compliance.
In one embodiment, an adapter apparatus for a respiratory therapy system having a pressure generating device and an electrical tube assembly, such as a heated tube assembly, coupled to a patient interface device. The adapter apparatus includes a first end having a first port member structured to be fluidly coupled to the electrical tube assembly, a second end having a second port member structured to receive a flow of breathing gas generated by the pressure generating device, the adapter apparatus being structured to deliver the flow of breathing gas to the electrical tube assembly through the first port member, and a wire assembly having a first electrical connector structured to be electrically coupled to the electrical tube assembly and a second electrical connector structured to be electrically coupled to the pressure generating device in order to provide an electrical connection between the electrical tube assembly and the pressure generating device.
In another embodiment, a respiratory therapy system is provided that includes a pressure generating device structured to generate a flow of breathing gas, a patient interface device, an electrical tube assembly coupled to the patient interface device, and an adapter apparatus as described above provided between the pressure generating device and the electrical tube assembly.
These and other objects, features, and characteristics of the present invention, as well as the methods of operation and functions of the related elements of structure and the combination of parts and economies of manufacture, will become more apparent upon consideration of the following description and the appended claims with reference to the accompanying drawings, all of which form a part of this specification, wherein like reference numerals designate corresponding parts in the various figures. It is to be expressly understood, however, that the drawings are for the purpose of illustration and description only and are not intended as a definition of the limits of the invention.
As used herein, the singular form of “a”, “an”, and “the” include plural references unless the context clearly dictates otherwise. As used herein, the statement that two or more parts or components are “coupled” shall mean that the parts are joined or operate together either directly or indirectly, i.e., through one or more intermediate parts or components, so long as a link occurs. As used herein, “directly coupled” means that two elements are directly in contact with each other. As used herein, “fixedly coupled” or “fixed” means that two components are coupled so as to move as one while maintaining a constant orientation relative to each other.
As used herein, the word “unitary” means a component is created as a single piece or unit. That is, a component that includes pieces that are created separately and then coupled together as a unit is not a “unitary” component or body. As employed herein, the statement that two or more parts or components “engage” one another shall mean that the parts exert a force against one another either directly or through one or more intermediate parts or components. As employed herein, the term “number” shall mean one or an integer greater than one (i.e., a plurality).
Directional phrases used herein, such as, for example and without limitation, top, bottom, left, right, upper, lower, front, back, and derivatives thereof, relate to the orientation of the elements shown in the drawings and are not limiting upon the claims unless expressly recited therein.
A system 2 adapted to provide a regimen of respiratory therapy to a patient according to one exemplary embodiment of the invention is generally shown in
Pressure generating device 4 is structured to generate a flow of breathing gas and may include, without limitation, ventilators, constant pressure support devices (such as a continuous positive airway pressure device, or CPAP device), variable pressure devices (e.g., BiPAP®, Bi-Flex®, or C-Flex™ devices manufactured and distributed by Philips Respironics of Murrysville, Pa.), and auto-titration pressure support devices. Delivery conduit assembly 6 is structured to communicate the flow of breathing gas from pressure generating device 4 to patient interface device 8. As described in more detail herein, delivery conduit assembly 6 is a heated delivery assembly that also allows for inclusion of an inline accessory 7 (such as, without limitation, an oxygen enrichment adapter, a pressure valve, a bacteria filter, or any other suitable accessory device that may be used in the patient circuit of a respiratory therapy device), shown schematically in
In the illustrated embodiment, patient interface 8 is a nasal/oral mask structured to cover the nose and mouth of the patient. However, any type of patient interface device 8, such as, without limitation, a nasal mask that covers the patient's nose, a nasal cushion having nasal prongs that are received within the patient's nares, or a full face mask that covers the patient's face, which facilitates the delivery of the flow of breathing gas to, and the removal of a flow of exhalation gas from, the airway of a patient may be used while remaining within the scope of the present invention. In the embodiment shown in
As seen in
Having described each of the individual parts of delivery conduit assembly 6, assembly of delivery conduit assembly 6 according to the exemplary embodiment will now be described. First, inline accessory adapter 24 is coupled to proximal end 36 of heated tube assembly 22. More specifically, tubular port member 66 of inline accessory adapter 24 is coupled to tubular port member 50 of heated tube assembly 22 and tab members 53 are inserted into slot member 63. In addition, electrical connector 54 of heated tube assembly 22 is coupled to first electrical connector 76 provided at the first end of cable member 74 of inline accessory adapter 24. Next, the first end of inline accessory 7 is fluidly coupled to tubular port member 70 of inline accessory adapter 24. In the non-limiting exemplary embodiment, inline accessory 7 has a male fitting 9 that is coupled to tubular port member 70. The second end of inline accessory 7 is then fluidly coupled to tubular port member 30 of outlet port 26. In the non-limiting exemplary embodiment, inline accessory 7 has a female fitting 11 that is coupled to tubular port member 30. As will be appreciated, this will result in heated tube assembly 22 being fluidly coupled to outlet port 26 of pressure generating device 4 through inline accessory adapter 24. Finally, second electrical connector 78 provided at the second end of cable member 74 of inline accessory adapter 24 is coupled to electrical connector 34 of outlet port 26. As will be appreciated, this will result in heating element 46 of heated tube assembly 22 being electrically coupled to outlet port 26 of pressure generating device 4 (and thus the power supply of pressure generating device 4) through inline accessory adapter 24.
Thus, inline accessory adapter 24 as just described provides an easy to use a mechanism for enabling the required electrical connection to be made between heated tube capable outlet port 26 and heated tube assembly 22 while simultaneously allowing inline accessory 7 to be inserted into the flow path to the user.
Enrichment adapter 80 includes a central adapter assembly 82 surrounded by a housing member 84.
Accordingly, enrichment adapter 80 as just described is a device that may be inserted in between heated tube assembly 22 and outlet port 26 which, when so inserted, simultaneously provides (i) a main fluid path from pressure generating device 4 to heated tube assembly 22, (ii) a secondary path by which supplemental gas may be introduced into the main flow path, and (iii) electrical connection to heated tube assembly 22 from outlet port 26 by way of a jumper in the form of wire harness assembly 98.
Furthermore, while in the illustrated embodiments inline accessory adapter 24 and enrichment adapter 80 are described as being used with heated tube assembly 22, it will be understood that the present invention is not limited to use with only heated tubes. Rather, inline accessory adapter 24 and enrichment adapter 80 may be used with any type of electrical tube assembly to which an electrical connection must be made, such as, without limitation, an electrical tube assembly that includes one or more wires for carrying an electrical signal from a patient interface device to a base unit and/or from a base unit to a patient interface device.
In the claims, any reference signs placed between parentheses shall not be construed as limiting the claim. The word “comprising” or “including” does not exclude the presence of elements or steps other than those listed in a claim. In a device claim enumerating several means, several of these means may be embodied by one and the same item of hardware. The word “a” or “an” preceding an element does not exclude the presence of a plurality of such elements. In any device claim enumerating several means, several of these means may be embodied by one and the same item of hardware. The mere fact that certain elements are recited in mutually different dependent claims does not indicate that these elements cannot be used in combination.
Although the invention has been described in detail for the purpose of illustration based on what is currently considered to be the most practical and preferred embodiments, it is to be understood that such detail is solely for that purpose and that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover modifications and equivalent arrangements that are within the spirit and scope of the appended claims. For example, it is to be understood that the present invention contemplates that, to the extent possible, one or more features of any embodiment can be combined with one or more features of any other embodiment.
Barclay, Mark Wayne, Bafile, Anthony Jon
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Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
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Jan 13 2014 | BAFILE, ANTHONY JON | KONINKLIJKE PHILIPS N V | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 035695 | /0223 | |
Jan 13 2014 | BARCLAY, MARK WAYNE | KONINKLIJKE PHILIPS N V | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 035695 | /0223 |
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